Inverse electron demand asymmetric cycloadditions of cyclic carbonyl ylides catalyzed by chiral Lewis acids—Scope and limitations of diazo and olefinic substrates-Reference-Cited by-同舟云学术

Inverse electron demand asymmetric cycloadditions of cyclic carbonyl ylides catalyzed by chiral Lewis acids—Scope and limitations of diazo and olefinic substrates

Published:2010-04 Issue:16 Volume:66 Page:3070-3089
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Suga Hiroyuki,Higuchi Satoshi,Ohtsuka Motoo,Ishimoto Daisuke,Arikawa Tadashi,Hashimoto Yuta,Misawa Shunta,Tsuchida Teruko,Kakehi Akikazu,Baba Toshihide

Funder

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference45 articles.

1. For books and reviewes, see:

2. Cascade Processes of Metallo Carbenoids

3. Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry toward Heterocycles and Natural Products,2003

4. Tandem cyclization-cycloaddition reaction of rhodium carbenoids. Scope and mechanistic details of the process

5. For representative examples, see

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